A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18134836



Internal ID20701876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:88545801..88546900hg38UCSC Ensembl
chr5:87841619..87842718hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6407102
Supporting Variants
Samples
Known GenesLINC00461
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18134836
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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